Issue 14, 2018

Thiacycle-fused benzo[1,2-b:4,5-b′]dithiophenes (BDTs): synthesis, packing, molecular orientation and semiconducting properties

Abstract

The molecular and packing structures of organic semiconductors play crucial roles in determining their charge carrier mobilities in organic field-effect transistors (OFETs). In this article, a systematic study on the functionalization of benzo[1,2-b:4,5-b′]dithiophene (BDT) with thiacycles to tune the packing, molecular orientation and semiconducting properties is reported. Among the designed BDT derivatives with six- or five-membered thiacycles containing sulphur atoms connected at the α-, β- or both α- and β-positions, the derivatives with β-sulphur atoms in the six-membered thiacycle exhibited a rubrene-like “pitched” π-stacking pattern and edge-on molecular orientation on the substrate. On the other hand, other derivatives exhibited different packing structures with a smaller intermolecular orbital overlap and end-on orientation. The thin-film OFETs based on the former molecules exhibited higher mobility than the latter, correlating the transport properties in the thin-film state with the position of the sulphur atoms and size of the thiacycles, which suggests novel molecular modification strategies in thienoacenes for the development of high performance semiconducting materials.

Graphical abstract: Thiacycle-fused benzo[1,2-b:4,5-b′]dithiophenes (BDTs): synthesis, packing, molecular orientation and semiconducting properties

Supplementary files

Article information

Article type
Paper
Submitted
20 ⵏⵓⵡ 2017
Accepted
14 ⴷⵓⵊ 2017
First published
09 ⵉⵏⵏ 2018

J. Mater. Chem. C, 2018,6, 3604-3612

Thiacycle-fused benzo[1,2-b:4,5-b′]dithiophenes (BDTs): synthesis, packing, molecular orientation and semiconducting properties

C. Wang, H. Nakamura, H. Sugino and K. Takimiya, J. Mater. Chem. C, 2018, 6, 3604 DOI: 10.1039/C7TC05317G

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